Canonical Allele Identifier: CA471133276

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604081A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844324A>C , CM000672.2:g.99844324A>C	GRCh38
NC_000010.10:g.101604081A>C , CM000672.1:g.101604081A>C	GRCh37
NC_000010.9:g.101594071A>C	NCBI36
NG_011798.1:g.66619A>C
NG_011798.2:g.66727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3846A>C MANE Select	ENSP00000497274.1:p.Ala1282=
ENST00000649459.1:n.194A>C
ENST00000370449.8:c.3846A>C	ENSP00000359478.4:p.Ala1282=
NM_000392.4:c.3846A>C	NP_000383.1:p.Ala1282=
XM_006717630.2:c.3150A>C	XP_006717693.1:p.Ala1050=
XR_945604.1:n.4035A>C
XR_945605.1:n.3910A>C
NM_000392.5:c.3846A>C MANE Select	NP_000383.2:p.Ala1282=
XM_006717630.3:c.3150A>C	XP_006717693.1:p.Ala1050=
XR_945604.3:n.4089A>C
XR_945605.3:n.3962A>C